A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504933



Internal ID20878197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25618638..25628088hg38UCSC Ensembl
chr16:25629959..25639409hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg389451
hg199451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029538
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer